Busch Lab

ZMP

ctnna2

Ensembl ID:
ENSDARG00000024785
ZFIN ID:
ZDB-GENE-060815-3
Description:
Catenin alpha-2 [Source:UniProtKB/Swiss-Prot;Acc:B7ZC77]
Human Orthologue:
CTNNA2
Human Description:
catenin (cadherin-associated protein), alpha 2 [Source:HGNC Symbol;Acc:2510]
Mouse Orthologue:
Ctnna2
Mouse Description:
catenin (cadherin associated protein), alpha 2 Gene [Source:MGI Symbol;Acc:MGI:88275]

Alleles

There are 8 alleles of this gene:

Allele Name Consequence Status Availability
sa16103 Nonsense Available for shipment Available now
sa32731 Nonsense Mutation detected in F1 DNA Not yet available
sa2006 Nonsense F2 line generated Not yet available
sa32732 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

This allele has been removed from public view.

Allele Name:
sa3343
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017139 Essential Splice Site 35 352 3 7
ENSDART00000101306 Essential Splice Site 35 865 3 17
ENSDART00000101311 Essential Splice Site 35 293 3 7
ENSDART00000110860 Essential Splice Site 35 373 2 7
ENSDART00000138740 Essential Splice Site 35 430 3 9
ENSDART00000143871 Essential Splice Site 22 271 2 5

The following transcripts of ENSDARG00000024785 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 42757425)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 41673741
GRCz11 1 42374905
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGWAGCCTTTGTACACAACAATCTTCATAGTTTGACTCTTTTTGTCCAC[A/T]GGTGACCACCCTGGTCAACACCWGCAACAAAGGCCCGTCCAGTAAGAAAA
Long Flanking Sequence:
TAGTAAATGTAGCCAGTGTTTAATTGAGAGATCATGAGGAGGTTTCCATCTTTGTATCAACATTTTCTTTGTAGCAGTTGAAGCAGCCAACGAAAATTTACGGACCTTTGCTTTTAAGGGAAATTGAGAGTTATCATTCAATAGTAACAAGATAACTTGTGTTTTTAATAAGGATGTTTTGAGGAGGTTCACACAGGACACATTCTTTCGGTTGACTGCATTATTTAATTGTAGATGGATGTCTTTGACTGTTGTGAGCGGCGGTCCCTTACCTGTTCATCATTCTGAAAGGAACAAACAAATCCAGCAGCTTCTTTCTGACCCACTGGTTCAGAAATAAACAACCTTAGACTTAATCATCTTTGTGTGCATCTCACTTTTTATTAGATGTGGCATTCAAACTAACGTTGCCAGATTCTACTTCATGCAGCTCTGTCAAAATGTGAACTAAAGTAGCCTTTGTACACAACAATCTTCATAGTTTGACTCTTTTTGTCCAC[A/T]GGTGACCACCCTGGTCAACACCAGCAACAAAGGCCCGTCCAGTAAGAAAAAGGGTCGCTCTAAGAAGGCTCATGTTTTGGCTGTGTCCGTGGAACAGGCCACCCAGAACTTTCTGGAAAAGGGTGAGCAGATTGCTAAGGACAGCCAGGACCTGAAAGAGGAGCTCATCGCAGCTGTAGAGGACGTCCGCAAGCAAGGTGAGCAGCCTGTTATTACCCTCAGGAACATCTCCAAAACAAAACCTGCTGCTTACTTGTTCTGGCGTCCCAAACATGTATATTAATGCGGTAAATGATTTATAACTCAGAGGAGGGTTTGACATCATGGATAAAGTTTTGTCTACAGGCCTGATTATTAGATGTGTTTGGTTACTTAAGAGAGAAGGAAAGACTTTGAGCAATGCTTGTCACATACATTTATCATTTACTTTTATGTTGTTGCAATGTATTTGTTCTAAAGCTGTGTTTTTATCACTGTTCTGTCAGATTTTATTTTGTTTT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa25637
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017139 Nonsense 188 352 5 7
ENSDART00000101306 None None 865 None 17
ENSDART00000101311 Nonsense 188 293 5 7
ENSDART00000110860 Nonsense 188 373 4 7
ENSDART00000138740 Nonsense 188 430 5 9
ENSDART00000143871 Nonsense 175 271 4 5

The following transcripts of ENSDARG00000024785 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 42770937)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 41687253
GRCz11 1 42388417
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGCCAACCGTTTTAAGGAGTTTGGGAAAGAGATGGTCAAACTCAACTA[T/A]GTTGCTGCTCGCAGACAGCAGGTATTATTAAACATCACACATTTTTGTTG
Long Flanking Sequence:
TTAGTTTTTATTATATATATTTTTTCCTTTTTTTTTTGCCCAGCGGCATCTGTTATATAATCACTAAACAAATTTGAAAAGCTAAGATCTGTGAAAGTTAATGGTTGTGAAAGAAGAACTTTTATAGTGTTGGATGTGGCTGAGAAACTTTTAGATGTCCCACAAGGGATACAACACCTCCCTGTTCTTCCGCTTGTTTCATTACGGAGACTGAAAACTGTCAGGATTTACATTAAATGTGCCCCAGGAGAGCCAATAATAAGCACTACAGAAGTGAGGCATCACTCAACCGCATAAAGTTGAAGTGCTTTAAGGAACTTTATACCTTCTTTTATTTTATGTTCATAGCATTTTGTGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTTCAGGTGGAAGAAGCTCTAGAAGCTGTTAAGAATGCTACCAACGAGCAGGACTTGGCCAACCGTTTTAAGGAGTTTGGGAAAGAGATGGTCAAACTCAACTA[T/A]GTTGCTGCTCGCAGACAGCAGGTATTATTAAACATCACACATTTTTGTTGATAAAATATATATATTATTATATAGTTTTATAATAATAACAATATTTCATTAGAGATTTGTTTACACCTTCAAAACATAATAAGAGAAAATAAGCAAAAATTAATGGGTGTAACACATTACAAAATAATACATACAACTATTAACTTAAACTATAAAAAGTATGGTTATAAACAACCTATATCTATGTAGGTTTGAACACCAACAAATATTGATTTAAACTAGCACATAATGTACAGCTCCCAGCAGGTACCTTGATGTCAAAACAATATCGAACTGACATCAAGCATAACATCAAAAAACACATCAAATAATGCAAATCGATTTGCTGTCAAAAGCTTGACGTCCATTTGACATCCACACACTGATGTCCTTTTGACCACCAAAATGAAGAAACAAAATTTATTATAATATGAGAACAGTTTTATTTATCTGGAATTCCAAATTCTGCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16103
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017139 None None 352 None 7
ENSDART00000101306 Nonsense 396 865 9 17
ENSDART00000101311 None None 293 None 7
ENSDART00000110860 None None 373 None 7
ENSDART00000138740 None None 430 None 9
ENSDART00000143871 None None 271 None 5

The following transcripts of ENSDARG00000024785 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 43362451)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 42278767
GRCz11 1 42979931
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTCACCAACATCATWCTTTCTGTGTTTTTCAGGTGGCCAACCTCGCCTG[T/A]TCCATCTCCAACAATGAGGAGGGGGTGAAGYTAGTGCGCATGGCTGCTAC
Long Flanking Sequence:
GGCCGCTAAAAATTCAAATTACACTGTGTGTGATGTCAATTATTCAAATAGATGCTATTTTTAAAAATAGTAAAAGAGAGACCAAGGCGGGATGATTTTGGGCCGGGGGAGCGCAGGGGACGAGGGACCCACAAATCATGTTCTTCACGCTGGGAAATAACAAATACCAATCTAACACTTGAATGAGCTCTAACTCTCTGTACATATTTTGCCCTGACATTGCCTTCTCAAGCCAAGCATTAAATCCTTATCCAATGCACACAGCACTGATAGCTTCAAACATGAACAGGGAAAAAGGACCACACGTTTGTGTATGTGCGCACTCTGCTTGAGAGCTTTATGTGCTTCCGTCCGAATGTTAGTCTAACCTGCTTGATTTACAGAAAAGCGGGCAACCGGAACCCCAAGGTCACTTTACACTTAAATCTAGACATACAAAATAACCCGATTGCTCACCAACATCATTCTTTCTGTGTTTTTCAGGTGGCCAACCTCGCCTG[T/A]TCCATCTCCAACAATGAGGAGGGGGTGAAGTTAGTGCGCATGGCTGCTACACAGATCGATAGCCTGTGTCCTCAGGTAAAAAGGCCAGAACCTTCTGCTATCCATCCAGTTTTCTACAACCTTTTGCAGCAGTTTTATGTGCTGTTGACAAATACCAATTTGTCACTTAGTTACTATAATGTACCTTATTTGCAAACACTCTATTTACTTAGCACCATTTGTCTGCCACAACTAACATTATGGCTTAATCAGCCACCCAAAGCACAGAGATTCCTTAAGAAGAGATGTTTGTGTACATTTGTTTTATTGACGATGGCGGCAGTTATTCTTCAAATGATGGAGAAGAGCATAGCCGGGTACATATTCAGATCTGTCACATGTATTAAATATGACTCGCATTACATTTTTTTAGCGATTCGGAGTCTACATGAAATTGCTTTTGCAACCCGCTGGAAAAAAATGGAAGGAATCAGTCAGAGGTAAAATCCACTGGGGACAGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32731
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017139 None None 352 None 7
ENSDART00000101306 Nonsense 414 865 9 17
ENSDART00000101311 None None 293 None 7
ENSDART00000110860 None None 373 None 7
ENSDART00000138740 None None 430 None 9
ENSDART00000143871 None None 271 None 5

The following transcripts of ENSDARG00000024785 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 43362503)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 42278819
GRCz11 1 42979983
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATCTCCAACAATGAGGAGGGGGTGAAGTTAGTGCGCATGGCTGCTACA[C/T]AGATCGATAGCCTGTGTCCTCAGGTAAAAAGGCCAGAACCTTCTGCTATC
Long Flanking Sequence:
TGCTATTTTTAAAAATAGTAAAAGAGAGACCAAGGCGGGATGATTTTGGGCCGGGGGAGCGCAGGGGACGAGGGACCCACAAATCATGTTCTTCACGCTGGGAAATAACAAATACCAATCTAACACTTGAATGAGCTCTAACTCTCTGTACATATTTTGCCCTGACATTGCCTTCTCAAGCCAAGCATTAAATCCTTATCCAATGCACACAGCACTGATAGCTTCAAACATGAACAGGGAAAAAGGACCACACGTTTGTGTATGTGCGCACTCTGCTTGAGAGCTTTATGTGCTTCCGTCCGAATGTTAGTCTAACCTGCTTGATTTACAGAAAAGCGGGCAACCGGAACCCCAAGGTCACTTTACACTTAAATCTAGACATACAAAATAACCCGATTGCTCACCAACATCATTCTTTCTGTGTTTTTCAGGTGGCCAACCTCGCCTGTTCCATCTCCAACAATGAGGAGGGGGTGAAGTTAGTGCGCATGGCTGCTACA[C/T]AGATCGATAGCCTGTGTCCTCAGGTAAAAAGGCCAGAACCTTCTGCTATCCATCCAGTTTTCTACAACCTTTTGCAGCAGTTTTATGTGCTGTTGACAAATACCAATTTGTCACTTAGTTACTATAATGTACCTTATTTGCAAACACTCTATTTACTTAGCACCATTTGTCTGCCACAACTAACATTATGGCTTAATCAGCCACCCAAAGCACAGAGATTCCTTAAGAAGAGATGTTTGTGTACATTTGTTTTATTGACGATGGCGGCAGTTATTCTTCAAATGATGGAGAAGAGCATAGCCGGGTACATATTCAGATCTGTCACATGTATTAAATATGACTCGCATTACATTTTTTTAGCGATTCGGAGTCTACATGAAATTGCTTTTGCAACCCGCTGGAAAAAAATGGAAGGAATCAGTCAGAGGTAAAATCCACTGGGGACAGGAAAAAAAAGATCTTGGGTTATGTTATATCATATGATAATTCATAATGTAGCC
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa4860
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017139 None None 352 None 7
ENSDART00000101306 Nonsense 585 865 12 17
ENSDART00000101311 None None 293 None 7
ENSDART00000110860 None None 373 None 7
ENSDART00000138740 None None 430 None 9
ENSDART00000143871 None None 271 None 5

The following transcripts of ENSDARG00000024785 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 43392043)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 42308359
GRCz11 1 43009523
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTTCATCGATGCCTCTCGCCTCGTCTACGATGGAGTGCGTGACAKCAGG[A/T]AAGCAGTCCTCATGATAAGAGTGAGTAATGGCCAAATAAAACCCCCRAGA
Long Flanking Sequence:
AAACCAGTTACAGTGTCTTACCCTTACCATGTTTAATTATTCCACCTGCTATGATAAAAGGCTATAAAATATCCTCAAATATAACCTACAGTATCAGCCAAGAGTCTTTCTGTACATAAACACACATGATGTAAAAGAGAACAGTGACCAAGTCCATATTTCTTATAACAACCTATCATTACCACTCATAGTATTACAAGCTTTGCATTGTGAAGTGTTTTATTTTGTTTAAATATGTTGTTTAGGTGTTTATACTTTTAATTTGGAACCTTTTTCTTGTTATGTACTTGCTCAACAAATTGATTGCTTTTTTGACCCATTTAAAAAATGTTGCAGCTTTATATCCTCTATGCTCTTCTTTCCCACCAGTGATGCCACGCTTTGCTGAGCAGGTTGAGGTGGCCATAGAGGCTCTGAGCACCAGCCCCCCGCAGCCATTTGAGGAAAACGAGTTCATCGATGCCTCTCGCCTCGTCTACGATGGAGTGCGTGACATCAGG[A/T]AAGCAGTCCTCATGATAAGAGTGAGTAATGGCCAAATAAAACCCCCAAGAGGTGCTCGATCTTCACTAGCGGGGCCTTTATTGTGCTTATTGCCCCAGAGCTTTGTATGATAAAAAGAAAATAACTTATTGAACATTTTTCATTTGCAAATAATGTAGTGGGGGAAAAATGCTGAAATTTACACAATTCTTTTATGTTGTCCTAACACAAATCGATTCAGTTATCTTAAAAGGCCCCTATTATGGGTTTTTGAAAATGACCTTCCCTCAAAGTGAAGTGAAATATCCAGCTAAAGCTTAAATCTGAAAGTGCATCGTGTTTAAAACTATTGACTCATCTATAAAAGAGTTGACTCCTAGTGGTTTGAATGAATTGTCGCTGTAACGACTCTTTAGCCATGTCGGCGTGACGTCATTTTTCTGACGAGTGCTTCAGCAATCTACATGCTTACAATTGGCATTTGTCAGCCGTTTGTTGAAGGACAGATCAGAAAAGACTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2006
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017139 None None 352 None 7
ENSDART00000101306 Nonsense 646 865 14 17
ENSDART00000101311 None None 293 None 7
ENSDART00000110860 None None 373 None 7
ENSDART00000138740 None None 430 None 9
ENSDART00000143871 None None 271 None 5
ENSDART00000017139 None None 352 None 7
ENSDART00000101306 Nonsense 646 865 14 17
ENSDART00000101311 None None 293 None 7
ENSDART00000110860 None None 373 None 7
ENSDART00000138740 None None 430 None 9
ENSDART00000143871 None None 271 None 5

The following transcripts of ENSDARG00000024785 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 43405283)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 42321599
GRCz11 1 43022763
KASP Assay ID:
554-3244.1 (used for ordering genotyping assays)
KASP Sequence:
AGGCCATCATGGCTCAGCTGCCTCAGGAAGAAAAGGCCAAGATTGCTGAA[C/T]AGGTCGAGAGCTTCAGGCAGGAAAAGAGCAAGCTGGACGCTGAAGTCGCT
Long Flanking Sequence:
TCCGTCCAGCCGCTCTGACAGAGCGTTGAACAAATGCATAATTCATTGACTGGTGTAAGAAGTGAGGTAATTATACATTTATCTCACAAATAATACTGCGCCTTAACAGTGCCTGTGACCTTGCAAAGAGATTAATGCCCTTTTGGACTGGCTCAGAATCGCTACGGAGCGAGAATTTATTCCTTGACAAGAAGAGGGGGAAAGAAAGGATGGATTTTCTCTTTATGAGCATGAGATGTCATGGGGTTCCAGAAGGTCTTATGATTAAGTGTTAAGTTTCAAAACCTTATACAGAGGCATTTCAGTGGGGTTAAACAAAGTCAGCCTAAATGGAGGGTACTTTCTTTACAAACTTTTAACTAGAATTAAGTGCATGTGTTGTGAAAAAGGCGAGATGTTCCTAATTGATCTTTTTTTTTTTTTTTCTTGTGCCATATTGCTATATCCCACAGGCCATCATGGCTCAGCTGCCTCAGGAAGAAAAGGCCAAGATTGCTGAA[C/T]AGGTCGAGAGCTTCAGGCAGGAAAAGAGCAAGCTGGACGCTGAAGTCGCTAAGTGGGATGACAATGGAAATGACATCATCGTGTTGGCTAAGCAGATGTGTATGATCATGATGGAGATGACTGACTTCACCAGGTACATCCGCACATTTTGAGTGTGGAAATGCTGGAAACATTTAATACAGGAAAATCCGAAGGGCTGTTGTCCTGTACATTTTAGCTCCAAAGCCAATTAGACCCACCTGAACCAGCTAATCAAGTTCTTACTGGGCATGCTAGAAACTTACTGGCAGCCGCTGAGGCAAGTTGGATCTTAACTTTGGAGGACATCAGCCCACCAAGATTGAGTTTGGGTACACTTGATTGAACAGAGAACCCTATATCTTAAATATTGCATGTCTATTTAATATATAAAAACATGGAGATTCAAACTTTAAAAGCTAAAATCTAATTAGCTTTTACTCTAGATGATTATATCAATATTTGAAAAGAATTTAAAGGTT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa5663
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017139 None None 352 None 7
ENSDART00000101306 Nonsense 646 865 14 17
ENSDART00000101311 None None 293 None 7
ENSDART00000110860 None None 373 None 7
ENSDART00000138740 None None 430 None 9
ENSDART00000143871 None None 271 None 5
ENSDART00000017139 None None 352 None 7
ENSDART00000101306 Nonsense 646 865 14 17
ENSDART00000101311 None None 293 None 7
ENSDART00000110860 None None 373 None 7
ENSDART00000138740 None None 430 None 9
ENSDART00000143871 None None 271 None 5

The following transcripts of ENSDARG00000024785 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 43405283)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 42321599
GRCz11 1 43022763
KASP Assay ID:
554-3244.1 (used for ordering genotyping assays)
KASP Sequence:
AGGCCATCATGGCTCAGCTGCCTCAGGAAGAAAAGGCCAAGATTGCTGAA[C/T]AGGTCGAGAGCTTCAGGCAGGAAAAGAGCAAGCTGGACGCTGAAGTCGCT
Long Flanking Sequence:
TCCGTCCAGCCGCTCTGACAGAGCGTTGAACAAATGCATAATTCATTGACTGGTGTAAGAAGTGAGGTAATTATACATTTATCTCACAAATAATACTGCGCCTTAACAGTGCCTGTGACCTTGCAAAGAGATTAATGCCCTTTTGGACTGGCTCAGAATCGCTACGGAGCGAGAATTTATTCCTTGACAAGAAGAGGGGGAAAGAAAGGATGGATTTTCTCTTTATGAGCATGAGATGTCATGGGGTTCCAGAAGGTCTTATGATTAAGTGTTAAGTTTCAAAACCTTATACAGAGGCATTTCAGTGGGGTTAAACAAAGTCAGCCTAAATGGAGGGTACTTTCTTTACAAACTTTTAACTAGAATTAAGTGCATGTGTTGTGAAAAAGGCGAGATGTTCCTAATTGATCTTTTTTTTTTTTTTTCTTGTGCCATATTGCTATATCCCACAGGCCATCATGGCTCAGCTGCCTCAGGAAGAAAAGGCCAAGATTGCTGAA[C/T]AGGTCGAGAGCTTCAGGCAGGAAAAGAGCAAGCTGGACGCTGAAGTCGCTAAGTGGGATGACAATGGAAATGACATCATCGTGTTGGCTAAGCAGATGTGTATGATCATGATGGAGATGACTGACTTCACCAGGTACATCCGCACATTTTGAGTGTGGAAATGCTGGAAACATTTAATACAGGAAAATCCGAAGGGCTGTTGTCCTGTACATTTTAGCTCCAAAGCCAATTAGACCCACCTGAACCAGCTAATCAAGTTCTTACTGGGCATGCTAGAAACTTACTGGCAGCCGCTGAGGCAAGTTGGATCTTAACTTTGGAGGACATCAGCCCACCAAGATTGAGTTTGGGTACACTTGATTGAACAGAGAACCCTATATCTTAAATATTGCATGTCTATTTAATATATAAAAACATGGAGATTCAAACTTTAAAAGCTAAAATCTAATTAGCTTTTACTCTAGATGATTATATCAATATTTGAAAAGAATTTAAAGGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32732
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017139 None None 352 None 7
ENSDART00000101306 Nonsense 677 865 14 17
ENSDART00000101311 None None 293 None 7
ENSDART00000110860 None None 373 None 7
ENSDART00000138740 None None 430 None 9
ENSDART00000143871 None None 271 None 5

The following transcripts of ENSDARG00000024785 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 1 (position 43405376)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 42321692
GRCz11 1 43022856
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTCGCTAAGTGGGATGACAATGGAAATGACATCATCGTGTTGGCTAAG[C/T]AGATGTGTATGATCATGATGGAGATGACTGACTTCACCAGGTACATCCGC
Long Flanking Sequence:
TACTGCGCCTTAACAGTGCCTGTGACCTTGCAAAGAGATTAATGCCCTTTTGGACTGGCTCAGAATCGCTACGGAGCGAGAATTTATTCCTTGACAAGAAGAGGGGGAAAGAAAGGATGGATTTTCTCTTTATGAGCATGAGATGTCATGGGGTTCCAGAAGGTCTTATGATTAAGTGTTAAGTTTCAAAACCTTATACAGAGGCATTTCAGTGGGGTTAAACAAAGTCAGCCTAAATGGAGGGTACTTTCTTTACAAACTTTTAACTAGAATTAAGTGCATGTGTTGTGAAAAAGGCGAGATGTTCCTAATTGATCTTTTTTTTTTTTTTTCTTGTGCCATATTGCTATATCCCACAGGCCATCATGGCTCAGCTGCCTCAGGAAGAAAAGGCCAAGATTGCTGAACAGGTCGAGAGCTTCAGGCAGGAAAAGAGCAAGCTGGACGCTGAAGTCGCTAAGTGGGATGACAATGGAAATGACATCATCGTGTTGGCTAAG[C/T]AGATGTGTATGATCATGATGGAGATGACTGACTTCACCAGGTACATCCGCACATTTTGAGTGTGGAAATGCTGGAAACATTTAATACAGGAAAATCCGAAGGGCTGTTGTCCTGTACATTTTAGCTCCAAAGCCAATTAGACCCACCTGAACCAGCTAATCAAGTTCTTACTGGGCATGCTAGAAACTTACTGGCAGCCGCTGAGGCAAGTTGGATCTTAACTTTGGAGGACATCAGCCCACCAAGATTGAGTTTGGGTACACTTGATTGAACAGAGAACCCTATATCTTAAATATTGCATGTCTATTTAATATATAAAAACATGGAGATTCAAACTTTAAAAGCTAAAATCTAATTAGCTTTTACTCTAGATGATTATATCAATATTTGAAAAGAATTTAAAGGTTGACCAGCGAATATTCCTTATAAAAGTTGTTCTTGTCTCAGAATAGAAAGTACAAAAGCTGTTTCTTGGGGTGGTATCCTTTTAAAGGGCACTA
Associated Phenotype:
Not determined